RS587776949 NDUFS4

Health Risk Chr 5:53683152
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial complex I deficiency
nuclear type 1
Leigh syndrome
Inborn genetic diseases
See cases
Mitochondrial complex I deficiency
nuclear type 1
Leigh syndrome
Inborn genetic diseases
See cases
Other Variants in NDUFS4
rs1445075330 rs121908985 rs104893898 rs104893899 rs138941073 rs73754255 rs185711494 rs149323691 rs760391381 rs200384843
Ask Dr. Hemsworth about this variant